Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2009-5-19
pubmed:abstractText
Cyclooxygenase (COX)-2 is a central enzyme of arachidonic acid metabolism, and its modulation by statins may explain some of the myocardial protective effects of these drugs. Dendritic cells (DCs) play a central role in microbial defense and in atherogenesis, and COX-2 expression in DCs is important for their migration to lymph nodes and antibody response, thus explaining why prostaglandin E(2) is a main component of the cocktails used to prepare DCs for clinical applications. On this basis, we addressed the effect of atorvastatin (ATV) on the release of arachidonic acid and on the expression of COX-2 in human monocyte-derived DCs. Although ATV on its own lacked any effect on COX-2 protein induction expression, it enhanced the release of arachidonic acid, the expression of COX-2 protein, and the production of prostaglandin E(2) induced by the fungal wall extract zymosan, and to a lower extent the effect of peptidoglycan. The effect on COX-2 protein was observed mainly 24 h after stimulation by zymosan and was not reverted by mevalonate, thus pointing to an effect unrelated to cholesterol metabolism. It is noteworthy that COX-2 protein showed a great stability, with a t((1/2)) of approximately 12 h, which was enhanced in the presence of ATV. In view of the important role played by COX-2 on DC function, these data indicate that ATV, by enhancing COX-2 stability, may increase DC function after infectious bouts and also counteract some of the risks associated with sustained inhibition of COX-2.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD, http://linkedlifedata.com/resource/pubmed/chemical/Arachidonic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Cycloheximide, http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 1, http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 2, http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone, http://linkedlifedata.com/resource/pubmed/chemical/Heptanoic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl-CoA..., http://linkedlifedata.com/resource/pubmed/chemical/Mevalonic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Peptidoglycan, http://linkedlifedata.com/resource/pubmed/chemical/Phospholipases A2, Cytosolic, http://linkedlifedata.com/resource/pubmed/chemical/Pyrroles, http://linkedlifedata.com/resource/pubmed/chemical/Zymosan, http://linkedlifedata.com/resource/pubmed/chemical/atorvastatin
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1521-0103
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
329
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
987-94
pubmed:meshHeading
pubmed-meshheading:19318593-Antigens, CD, pubmed-meshheading:19318593-Arachidonic Acid, pubmed-meshheading:19318593-Cycloheximide, pubmed-meshheading:19318593-Cyclooxygenase 1, pubmed-meshheading:19318593-Cyclooxygenase 2, pubmed-meshheading:19318593-Dendritic Cells, pubmed-meshheading:19318593-Dinoprostone, pubmed-meshheading:19318593-Gene Expression, pubmed-meshheading:19318593-Half-Life, pubmed-meshheading:19318593-Heptanoic Acids, pubmed-meshheading:19318593-Humans, pubmed-meshheading:19318593-Hydroxymethylglutaryl-CoA Reductase Inhibitors, pubmed-meshheading:19318593-Kinetics, pubmed-meshheading:19318593-Mevalonic Acid, pubmed-meshheading:19318593-Peptidoglycan, pubmed-meshheading:19318593-Phospholipases A2, Cytosolic, pubmed-meshheading:19318593-Pyrroles, pubmed-meshheading:19318593-Zymosan
pubmed:year
2009
pubmed:articleTitle
Cyclooxygenase-2 induced by zymosan in human monocyte-derived dendritic cells shows high stability, and its expression is enhanced by atorvastatin.
pubmed:affiliation
Instituto de Biología y Genética Molecular, Consejo Superior de Investigaciones Científicas and Universidad de Valladolid, Spain.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't